Paucker K, Berman B J, Golgher R R, Stancek D
J Virol. 1970 Feb;5(2):145-52. doi: 10.1128/JVI.5.2.145-152.1970.
Under optimal conditions which minimized the accumulation of extraneous proteins, interferon preparations were obtained in L cells containing from 2 x 10(4) to 5 x 10(4) units/mg of protein. The radiolabeled proteins were liberated simultaneously with interferon from cultures exposed to tritiated amino acids after viral stimulation and from corresponding controls, and were subsequently purified with the following results. Chromatography of interferon on carboxymethyl-Sephadex C-25 eliminated selectively unlabeled or poorly labeled proteins, resulting in a greater than sixfold increase in counts per minute per milligram of protein. Similarly purified control material harbored at least 12 times less tritium per milligram of protein than interferon, and the label was more diversely distributed among proteins of different molecular weights. On electrophoresis of interferon in polyacrylamide gels, labeled proteins were reduced further by a factor of at least 10 without loss in titer. Final purification was estimated at greater than 280-fold, representing a calculated specific activity of at least 1.4 x 10(7) units of interferon per milligram of protein.
在将无关蛋白质积累降至最低的最佳条件下,在每毫克蛋白质含2×10⁴至5×10⁴单位的L细胞中获得了干扰素制剂。在病毒刺激后,放射性标记的蛋白质与干扰素同时从暴露于氚化氨基酸的培养物以及相应对照中释放出来,随后进行纯化,结果如下。干扰素在羧甲基 - 葡聚糖凝胶C - 25上的色谱分离选择性地去除了未标记或标记不佳的蛋白质,导致每毫克蛋白质的每分钟计数增加了六倍以上。同样纯化的对照物质每毫克蛋白质所含的氚比干扰素至少少12倍,并且标记在不同分子量的蛋白质中分布更为分散。在聚丙烯酰胺凝胶中对干扰素进行电泳时,标记的蛋白质进一步减少了至少10倍,而效价没有损失。最终纯化估计超过280倍,这表明每毫克蛋白质的干扰素比活性至少为1.4×10⁷单位。